tailieunhanh - Birt–Hogg–Dubé syndrome: A literature review and case study of a Chinese woman presenting a novel FLCN mutation

The Birt–Hogg–Dubé (BHD) syndrome is a very rare autosomal dominant form of genodermatosis caused by germline mutations in the folliculin (FLCN) gene, which is mapped to the region in chromosome 17. |

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